Full Name
Hope Rugo, MD
Speaker Bio
Hope S. Rugo, M.D., is division chief of breast medical oncology and a professor of medical oncology and therapeutics research at City of Hope®. She also serves as director of the Women’s Cancers Program for City of Hope’s national network of cancer centers.
A world-renowned expert in breast cancer and clinical trial design and execution, Dr. Rugo oversees all women’s cancer research initiatives and clinical care at City of Hope. She is focused on expanding clinical trials, advancing translational research, and standardizing care to improve patient outcomes. She is deeply committed to improving access to innovative new therapies for breast cancer patients everywhere and takes a compassionate, collaborative approach in her work.
Dr. Rugo has been directly involved in numerous projects that have established new standards of care for breast cancer. She has served on the steering committees of multiple clinical trials that led to the approval of agents such as PARP inhibitors, CDK4/6 inhibitors, PI3K inhibitors, checkpoint inhibitors, and antibody-drug conjugates, among others. Additionally, Dr. Rugo has led several studies aimed at minimizing therapy-related toxicity, contributing to the U.S. Food and Drug Administration’s approval of scalp cooling caps to prevent chemotherapy-induced hair loss and a steroid mouthwash to alleviate stomatitis caused by targeted therapies. She also served as co-chair of the Triple Negative Working Group of the Translational Breast Cancer Research Consortium, where she spearheaded groundbreaking multicenter clinical trials in collaboration with researchers, pharmaceutical companies, and clinical providers.
As a physician-scholar with more than 500 peer-reviewed publications, Dr. Rugo served on the editorial board of the American Society of Clinical Oncology's Education Committee, which included co-chairing the creation of new guidelines for the hormonal treatment of metastatic breast cancer. She is an Associated editor for the ASCO meeting annual educational manuscripts, committed to educating patients and medical provider on the latest in breast cancer treatment. Dr. Rugo has presented on her work at conferences around the world. Along the way, she's been recognized with numerous awards, including the Bank of America Gianini Foundation Award and the European Society for Medical Oncology's 2024 Breast Cancer Award.
A world-renowned expert in breast cancer and clinical trial design and execution, Dr. Rugo oversees all women’s cancer research initiatives and clinical care at City of Hope. She is focused on expanding clinical trials, advancing translational research, and standardizing care to improve patient outcomes. She is deeply committed to improving access to innovative new therapies for breast cancer patients everywhere and takes a compassionate, collaborative approach in her work.
Dr. Rugo has been directly involved in numerous projects that have established new standards of care for breast cancer. She has served on the steering committees of multiple clinical trials that led to the approval of agents such as PARP inhibitors, CDK4/6 inhibitors, PI3K inhibitors, checkpoint inhibitors, and antibody-drug conjugates, among others. Additionally, Dr. Rugo has led several studies aimed at minimizing therapy-related toxicity, contributing to the U.S. Food and Drug Administration’s approval of scalp cooling caps to prevent chemotherapy-induced hair loss and a steroid mouthwash to alleviate stomatitis caused by targeted therapies. She also served as co-chair of the Triple Negative Working Group of the Translational Breast Cancer Research Consortium, where she spearheaded groundbreaking multicenter clinical trials in collaboration with researchers, pharmaceutical companies, and clinical providers.
As a physician-scholar with more than 500 peer-reviewed publications, Dr. Rugo served on the editorial board of the American Society of Clinical Oncology's Education Committee, which included co-chairing the creation of new guidelines for the hormonal treatment of metastatic breast cancer. She is an Associated editor for the ASCO meeting annual educational manuscripts, committed to educating patients and medical provider on the latest in breast cancer treatment. Dr. Rugo has presented on her work at conferences around the world. Along the way, she's been recognized with numerous awards, including the Bank of America Gianini Foundation Award and the European Society for Medical Oncology's 2024 Breast Cancer Award.
Speaking At
GS1-01 - KEYNOTE-522 Study of Neoadjuvant Pembrolizumab + Chemotherapy vs Placebo + Chemotherapy, Followed by Adjuvant Pembrolizumab vs Placebo for Early-Stage TNBC: Event-Free Survival Sensitivity and Subgroup Analyses
GS1-02 - Efficacy of Pembrolizumab + Chemotherapy vs Placebo + Chemotherapy by PD-L1 Combined Positive Score 1-9, 10-19, and ≥20 for Previously Untreated Locally Recurrent Inoperable or Metastatic Triple-Negative Breast Cancer
GS1-05 - Datopotamab Deruxtecan (Dato-DXd) in Advanced/Metastatic HER2 Negative Breast Cancer: Triple Negative Breast Cancer Results from the Phase 1 TROPION-PanTumor01 Study
GS1-08 - CCTG MA.32 A Phase Ill Randomized Trial of the Effect of Metformin versus Placebo on Recurrence and Survival in Early-Stage Breast Cancer
GS1-10 - Clinical utility of genomic profiling in patients with metastatic breast cancer: Results of a randomized trial
GS3-04A - Capivasertib and fulvestrant for patients with aromatase inhibitor-resistant hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer: Results from the Phase III CAPItello-291 trial
GS3-04A - Capivasertib and fulvestrant for patients with aromatase inhibitor-resistant hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer: Results from the Phase III CAPItello-291 trial
GS3-06 - PACE: Palbociclib After CDK and Endocrine Therapy A Randomized Phase I| Study of Fulvestrant +/ - Palbociclib after Progression on CDK4/6 inhibitor for HR+/HER2- Metastatic Breast Cancer
GS1-10 - Primary Results From the Randomized Phase Il RIGHT Choice Trial of Premenopausal Patients With Aggressive HR+/HER2- Advanced Breast Cancer Treated With Ribociclib + Endocrine Therapy vs Physician's Choice Combination Chemotherapy
GS1-11 - Sacituzumab Govitecan vs Treatment of Physician's Choice: Efficacy by Trop-2 Expression in the TROPiCS-02 Study of Patients With HR+/HER2- Metastatic Breast Cancer
GS3-02 - Camizestrant, a next-generation oral SERD vs fulvestrant in post-menopausal women with advanced ER-positive HER2-negative breast cancer: Results of the randomized, multi-dose Phase 2 SERENA-2 trial
GS3-03 - ARV-471, a PROTAC® estrogen receptor (ER) degrader in advanced ER-positive/human epidermal growth factor receptor 2 (HER2)-negative breast cancer: phase 2 expansion (VERITAC) of a phase 1/2 study
HER2LOW - Low HER2- A separate entity? Published Data and SABCS News: a pathologist's perspective
GS01-01 - Biomarker results in high-risk estrogen receptor positive, human epidermal growth factor receptor 2 negative primary breast cancer following neoadjuvant chemotherapy ± nivolumab: An exploratory analysis of CheckMate 7FL
GS01-02 - Phase 3 study of neoadjuvant pembrolizumab or placebo plus chemotherapy, followed by adjuvant pembrolizumab or placebo plus endocrine therapy for early-stage high-risk ER+/HER2 - breast cancer: KEYNOTE-756
GS01-03 - Adding atezolizumab to adjuvant chemotherapy for stage II and III triple-negative breast cancer is unlikely to improve efficacy:interim analysis of the ALEXANDRA/IMpassion030 phase 3 trial.
GS01-05 - Pembrolizumab + olaparib vs pembrolizumab + chemotherapy after induction with pembrolizumab + chemotherapy for locally recurrent inoperable or metastatic TNBC: Randomized open-label phase 2 KEYLYNK-009 study
GS01-06 - Advancing evidence of the associations between specific benign breast diagnoses and future breast cancer risk
GS01-08 - CDK4/6 inhibition is a potential vulnerability in NF1-depleted ER+ breast cancer
GS01-10 - HER2CLIMB-02: Randomized, double-blind phase 3 trial of tucatinib and trastuzumab emtansine for previously treated her2-positive metastatic breast cancer
GS01-12 - MONARCH 3: Final overall survival results of abemaciclib plus a nonsteroidal aromatase inhibitor as first-line therapy for HR+, HER2- advanced breast cancer
GGS01-10 - HER2CLIMB-02: Randomized, double-blind phase 3 trial of tucatinib and trastuzumab emtansine for previously treated her2-positive metastatic breast cancer (China)
GS01-01 - Biomarker results in high-risk estrogen receptor positive, human epidermal growth factor receptor 2 negative primary breast cancer following neoadjuvant chemotherapy ± nivolumab: An exploratory analysis of CheckMate 7FL (China)
GS01-02 - Phase 3 study of neoadjuvant pembrolizumab or placebo plus chemotherapy, followed by adjuvant pembrolizumab or placebo plus endocrine therapy for early-stage high-risk ER+/HER2 - breast cancer: KEYNOTE-756 (China)
GS01-03 - Adding atezolizumab to adjuvant chemotherapy for stage II and III triple-negative breast cancer is unlikely to improve efficacy:interim analysis of the ALEXANDRA/IMpassion030 phase 3 trial. (China)
GS01-05 - Pembrolizumab + olaparib vs pembrolizumab + chemotherapy after induction with pembrolizumab + chemotherapy for locally recurrent inoperable or metastatic TNBC: Randomized open-label phase 2 KEYLYNK-009 study (China)
GS01-06 - Advancing evidence of the associations between specific benign breast diagnoses and future breast cancer risk (China)
GS01-08 - CDK4/6 inhibition is a potential vulnerability in NF1-depleted ER+ breast cancer (China)
GS01-12 - MONARCH 3: Final overall survival results of abemaciclib plus a nonsteroidal aromatase inhibitor as first-line therapy for HR+, HER2- advanced breast cancer (China)
GS3-01: Circulating tumor DNA surveillance in ZEST, a randomized, phase 3, double-blind study of niraparib or placebo in patients w/ triple-negative breast cancer or HER2+ BRCA-mutated breast cancer with molecular residual disease.
GS3-04: (Neo)adjuvant nab-PAC weekly vs sb-PAC q2w, followed by EC q2w, in genomically or clinically high-risk HR+/HER- early breast cancer according to ET-response: final survival results from the WSG ADAPT-HR+/HER2- chemotherapy-trial.
GS3-06: Neoadjuvant camrelizumab plus chemotherapy (chemo) for early or locally advanced triple-negative breast cancer (TNBC): a randomized, double-blind, phase 3 trial.
NSABP B-59/GBG-96-GeparDouze: A randomized double-blind phase III clinical trial of neoadjuvant chemotherapy with atezolizumab or placebo followed by adjuvant atezolizumab or placebo in patients with Stage II and III triple-negative breast cancer.
GS3-01 - Circulating tumor DNA surveillance in ZEST, a randomized, phase 3, double-blind study of niraparib or placebo in patients w/ triple-negative BC or HER2+ BRCA-mutated breast cancer with molecular residual disease after definitive therapy. (China)
GS3-05 - NSABP B-59/GBG-96-GeparDouze: A randomized double-blind phase III clinical trial of neoadjuvant chemotherapy with atezolizumab or placebo followed by adjuvant atezolizumab or placebo in patients with Stage II and III triple-negative BC. (China)
GS3-06 - Neoadjuvant camrelizumab plus chemotherapy (chemo) for early or locally advanced triple-negative breast cancer (TNBC): a randomized, double-blind, phase 3 trial. (China)
GS1-02 - Efficacy of Pembrolizumab + Chemotherapy vs Placebo + Chemotherapy by PD-L1 Combined Positive Score 1-9, 10-19, and ≥20 for Previously Untreated Locally Recurrent Inoperable or Metastatic Triple-Negative Breast Cancer
GS1-05 - Datopotamab Deruxtecan (Dato-DXd) in Advanced/Metastatic HER2 Negative Breast Cancer: Triple Negative Breast Cancer Results from the Phase 1 TROPION-PanTumor01 Study
GS1-08 - CCTG MA.32 A Phase Ill Randomized Trial of the Effect of Metformin versus Placebo on Recurrence and Survival in Early-Stage Breast Cancer
GS1-10 - Clinical utility of genomic profiling in patients with metastatic breast cancer: Results of a randomized trial
GS3-04A - Capivasertib and fulvestrant for patients with aromatase inhibitor-resistant hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer: Results from the Phase III CAPItello-291 trial
GS3-04A - Capivasertib and fulvestrant for patients with aromatase inhibitor-resistant hormone receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer: Results from the Phase III CAPItello-291 trial
GS3-06 - PACE: Palbociclib After CDK and Endocrine Therapy A Randomized Phase I| Study of Fulvestrant +/ - Palbociclib after Progression on CDK4/6 inhibitor for HR+/HER2- Metastatic Breast Cancer
GS1-10 - Primary Results From the Randomized Phase Il RIGHT Choice Trial of Premenopausal Patients With Aggressive HR+/HER2- Advanced Breast Cancer Treated With Ribociclib + Endocrine Therapy vs Physician's Choice Combination Chemotherapy
GS1-11 - Sacituzumab Govitecan vs Treatment of Physician's Choice: Efficacy by Trop-2 Expression in the TROPiCS-02 Study of Patients With HR+/HER2- Metastatic Breast Cancer
GS3-02 - Camizestrant, a next-generation oral SERD vs fulvestrant in post-menopausal women with advanced ER-positive HER2-negative breast cancer: Results of the randomized, multi-dose Phase 2 SERENA-2 trial
GS3-03 - ARV-471, a PROTAC® estrogen receptor (ER) degrader in advanced ER-positive/human epidermal growth factor receptor 2 (HER2)-negative breast cancer: phase 2 expansion (VERITAC) of a phase 1/2 study
HER2LOW - Low HER2- A separate entity? Published Data and SABCS News: a pathologist's perspective
GS01-01 - Biomarker results in high-risk estrogen receptor positive, human epidermal growth factor receptor 2 negative primary breast cancer following neoadjuvant chemotherapy ± nivolumab: An exploratory analysis of CheckMate 7FL
GS01-02 - Phase 3 study of neoadjuvant pembrolizumab or placebo plus chemotherapy, followed by adjuvant pembrolizumab or placebo plus endocrine therapy for early-stage high-risk ER+/HER2 - breast cancer: KEYNOTE-756
GS01-03 - Adding atezolizumab to adjuvant chemotherapy for stage II and III triple-negative breast cancer is unlikely to improve efficacy:interim analysis of the ALEXANDRA/IMpassion030 phase 3 trial.
GS01-05 - Pembrolizumab + olaparib vs pembrolizumab + chemotherapy after induction with pembrolizumab + chemotherapy for locally recurrent inoperable or metastatic TNBC: Randomized open-label phase 2 KEYLYNK-009 study
GS01-06 - Advancing evidence of the associations between specific benign breast diagnoses and future breast cancer risk
GS01-08 - CDK4/6 inhibition is a potential vulnerability in NF1-depleted ER+ breast cancer
GS01-10 - HER2CLIMB-02: Randomized, double-blind phase 3 trial of tucatinib and trastuzumab emtansine for previously treated her2-positive metastatic breast cancer
GS01-12 - MONARCH 3: Final overall survival results of abemaciclib plus a nonsteroidal aromatase inhibitor as first-line therapy for HR+, HER2- advanced breast cancer
GGS01-10 - HER2CLIMB-02: Randomized, double-blind phase 3 trial of tucatinib and trastuzumab emtansine for previously treated her2-positive metastatic breast cancer (China)
GS01-01 - Biomarker results in high-risk estrogen receptor positive, human epidermal growth factor receptor 2 negative primary breast cancer following neoadjuvant chemotherapy ± nivolumab: An exploratory analysis of CheckMate 7FL (China)
GS01-02 - Phase 3 study of neoadjuvant pembrolizumab or placebo plus chemotherapy, followed by adjuvant pembrolizumab or placebo plus endocrine therapy for early-stage high-risk ER+/HER2 - breast cancer: KEYNOTE-756 (China)
GS01-03 - Adding atezolizumab to adjuvant chemotherapy for stage II and III triple-negative breast cancer is unlikely to improve efficacy:interim analysis of the ALEXANDRA/IMpassion030 phase 3 trial. (China)
GS01-05 - Pembrolizumab + olaparib vs pembrolizumab + chemotherapy after induction with pembrolizumab + chemotherapy for locally recurrent inoperable or metastatic TNBC: Randomized open-label phase 2 KEYLYNK-009 study (China)
GS01-06 - Advancing evidence of the associations between specific benign breast diagnoses and future breast cancer risk (China)
GS01-08 - CDK4/6 inhibition is a potential vulnerability in NF1-depleted ER+ breast cancer (China)
GS01-12 - MONARCH 3: Final overall survival results of abemaciclib plus a nonsteroidal aromatase inhibitor as first-line therapy for HR+, HER2- advanced breast cancer (China)
GS3-01: Circulating tumor DNA surveillance in ZEST, a randomized, phase 3, double-blind study of niraparib or placebo in patients w/ triple-negative breast cancer or HER2+ BRCA-mutated breast cancer with molecular residual disease.
GS3-04: (Neo)adjuvant nab-PAC weekly vs sb-PAC q2w, followed by EC q2w, in genomically or clinically high-risk HR+/HER- early breast cancer according to ET-response: final survival results from the WSG ADAPT-HR+/HER2- chemotherapy-trial.
GS3-06: Neoadjuvant camrelizumab plus chemotherapy (chemo) for early or locally advanced triple-negative breast cancer (TNBC): a randomized, double-blind, phase 3 trial.
NSABP B-59/GBG-96-GeparDouze: A randomized double-blind phase III clinical trial of neoadjuvant chemotherapy with atezolizumab or placebo followed by adjuvant atezolizumab or placebo in patients with Stage II and III triple-negative breast cancer.
GS3-01 - Circulating tumor DNA surveillance in ZEST, a randomized, phase 3, double-blind study of niraparib or placebo in patients w/ triple-negative BC or HER2+ BRCA-mutated breast cancer with molecular residual disease after definitive therapy. (China)
GS3-05 - NSABP B-59/GBG-96-GeparDouze: A randomized double-blind phase III clinical trial of neoadjuvant chemotherapy with atezolizumab or placebo followed by adjuvant atezolizumab or placebo in patients with Stage II and III triple-negative BC. (China)
GS3-06 - Neoadjuvant camrelizumab plus chemotherapy (chemo) for early or locally advanced triple-negative breast cancer (TNBC): a randomized, double-blind, phase 3 trial. (China)
